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Molecular cloning, tissue expression, and transcriptional regulation of fabp1 and fabp2 in javelin goby (Synechogobius hasta) in response to starvation stress.
Chen, Xiangning; Gao, Yingli; Wu, Guanju; Gu, Jiaze; Cai, Yuefeng; Xu, Jianhe; Cheng, Hanliang.
Afiliação
  • Chen X; Jiangsu Key Laboratory of Marine Biotechnology, Jiangsu Ocean University, Lianyungang 222005, China; Jiangsu Key Laboratory of Marine Bioresources and Environment, Jiangsu Ocean University, Lianyungang 222005, China; Co-Innovation Center of Jiangsu Marine Bio-industry Technology, Lianyungang 222005,
  • Gao Y; Jiangsu Key Laboratory of Marine Biotechnology, Jiangsu Ocean University, Lianyungang 222005, China; Jiangsu Key Laboratory of Marine Bioresources and Environment, Jiangsu Ocean University, Lianyungang 222005, China; Co-Innovation Center of Jiangsu Marine Bio-industry Technology, Lianyungang 222005,
  • Wu G; College of Marine Science and Fisheries, Jiangsu Ocean University, Lianyungang 222005, China.
  • Gu J; College of Marine Science and Fisheries, Jiangsu Ocean University, Lianyungang 222005, China.
  • Cai Y; College of Marine Science and Fisheries, Jiangsu Ocean University, Lianyungang 222005, China.
  • Xu J; College of Marine Science and Fisheries, Jiangsu Ocean University, Lianyungang 222005, China.
  • Cheng H; College of Marine Science and Fisheries, Jiangsu Ocean University, Lianyungang 222005, China.
Article em En | MEDLINE | ID: mdl-32745520
ABSTRACT
Fatty acid binding proteins (FABPs) are intracellular lipid chaperones with low molecular weight, which are widely distributed in a variety of tissues, participating in fatty acid transport, cell proliferation, and angiogenesis. In this study, full-length sequences of two fabp genes (fabp1 and fabp2) from javelin goby (Synechogobius hasta) were cloned via RACE PCR, followed by bioinformatic analyses and gene expression evaluation. The fabp1 and fabp2 cDNA sequences were 493 and 626 bp in length, encoding 126 and 132 amino acids, respectively. Phylogenetic analysis revealed that both genes from S. hasta were clustered with those of other fish species in accordance with their known taxonomic relationships. fabp1 and fabp2 mRNA showed distinct expression patterns in different tissues, with fabp1 being most expressed in the liver and fabp2 in the intestine. Furthermore, the expression of fabp1 in the liver was significantly up-regulated during starvation, whereas fabp2 mRNA level in the intestine initially increased and then decreased, indicating that the transcriptional responses of the two genes could be influenced by malnourishment/starvation. Changes in the transcriptional levels of fabp1 and fabp2 also suggested that glycogen was catabolized in the liver of S. hasta at the beginning of starvation prior to lipid depletion, whereas lipids served as fuel reserves in the intestine during short-term starvation. In conclusion, this study provides fundamental insights into the role of Fabps in S. hasta lipid metabolism.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inanição / Estresse Fisiológico / Transcrição Gênica / Perciformes / Regulação da Expressão Gênica / Proteínas de Peixes / Proteínas de Ligação a Ácido Graxo Limite: Animals Idioma: En Revista: Comp Biochem Physiol B Biochem Mol Biol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inanição / Estresse Fisiológico / Transcrição Gênica / Perciformes / Regulação da Expressão Gênica / Proteínas de Peixes / Proteínas de Ligação a Ácido Graxo Limite: Animals Idioma: En Revista: Comp Biochem Physiol B Biochem Mol Biol Ano de publicação: 2020 Tipo de documento: Article